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4-Nitro-benzaldehyde-(O-acetyl-seqcis-oxime) is a complex organic chemical compound with the molecular formula C9H8N2O5. It is derived from 4-nitro-benzaldehyde, where an oxime group is attached to the aldehyde carbon, and an acetyl group is present on the oxygen atom of the oxime. The "seqcis" in the name suggests that the compound has a specific stereochemistry, with the oxime and acetyl groups arranged in a sequential cis configuration. 4-nitro-benzaldehyde-(O-acetyl-seqcis-oxime ) is often used in the synthesis of various pharmaceuticals and organic compounds due to its reactive functional groups, which can participate in a range of chemical reactions. It is important to handle such compounds with care, as they may have specific safety and toxicity profiles.

3848-34-8

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3848-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3848-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3848-34:
(6*3)+(5*8)+(4*4)+(3*8)+(2*3)+(1*4)=108
108 % 10 = 8
So 3848-34-8 is a valid CAS Registry Number.

3848-34-8Relevant academic research and scientific papers

EFFETS MICELLAIRES SUR LA BASICITE ET LA REACTIVITE DE NUCLEOPHILES α AROMATIQUES

Meyer, G.,Viout, P.

, p. 2269 - 2272 (1981)

The oximation of p-nitrophenylacetate by benzaldoximates in aqueous solution is catalyzed by CTAB micelles.The catalysis is more effective when the base strength of the oximate decreases; the reactivity of benzaldoximates is not dependent on their basicity.Our data may be interpreted in terms of orbital-controlled reactions, with interactions between both the n and ? occupied orbitals of the oximates and the LUMO of the acetate.

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